Risk Factors for Nab-Paclitaxel and Gemcitabine-Induced Peripheral Neuropathy in Patients with Pancreatic Cancer
Background: Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most frequent adverse events observed with taxane use, whose disability often required modification or treatment discontinuation. The aim of this study was to assess the value of several variables as risk factors for CIPN de...
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Veröffentlicht in: | Oncology 2022-07, Vol.100 (7), p.384-391 |
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description | Background: Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most frequent adverse events observed with taxane use, whose disability often required modification or treatment discontinuation. The aim of this study was to assess the value of several variables as risk factors for CIPN development. Material and Methods: Eligible patients with metastatic pancreatic cancer receiving chemotherapy with nab-paclitaxel and gemcitabine were assessed in a multicenter study. Peripheral neuropathy was categorized using the National Cancer Institute Common Toxicity Criteria scale, version 4.02, and a physical/neurological examination. Univariate and multivariate regression analyses were used to identify blood-based and clinical factors associated with CIPN. Results: Data were available from 153 patients from five Italian centers. Key risk factors of CIPN in univariate regression models included age, number of chemotherapy cycles, statin assumption, and concomitant comorbidities. However, in the multivariate analysis, only for age (OR 1.0, p < 0.01, 95% CI: 1.01–1.11) and the number of cycles (OR 1.22, p < 0.01, 95% CI: 1.09–1.36), the correlation with CIPN development has been confirmed. Conclusion: Our study confirms age and the number of chemotherapy cycles as CIPN risk factors. The identification and validation of different risk factors could be advantageous to prevent or optimize management of CIPN which outstandingly affect the patient’s quality of life. |
doi_str_mv | 10.1159/000524868 |
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The aim of this study was to assess the value of several variables as risk factors for CIPN development. Material and Methods: Eligible patients with metastatic pancreatic cancer receiving chemotherapy with nab-paclitaxel and gemcitabine were assessed in a multicenter study. Peripheral neuropathy was categorized using the National Cancer Institute Common Toxicity Criteria scale, version 4.02, and a physical/neurological examination. Univariate and multivariate regression analyses were used to identify blood-based and clinical factors associated with CIPN. Results: Data were available from 153 patients from five Italian centers. Key risk factors of CIPN in univariate regression models included age, number of chemotherapy cycles, statin assumption, and concomitant comorbidities. However, in the multivariate analysis, only for age (OR 1.0, p < 0.01, 95% CI: 1.01–1.11) and the number of cycles (OR 1.22, p < 0.01, 95% CI: 1.09–1.36), the correlation with CIPN development has been confirmed. Conclusion: Our study confirms age and the number of chemotherapy cycles as CIPN risk factors. The identification and validation of different risk factors could be advantageous to prevent or optimize management of CIPN which outstandingly affect the patient’s quality of life.</description><identifier>ISSN: 0030-2414</identifier><identifier>EISSN: 1423-0232</identifier><identifier>DOI: 10.1159/000524868</identifier><identifier>PMID: 35551139</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Albumins ; Antineoplastic Agents - adverse effects ; Care and treatment ; Clinical Study ; Complications and side effects ; Deoxycytidine - analogs & derivatives ; Gemcitabine ; Humans ; Paclitaxel ; Paclitaxel - adverse effects ; Pancreatic cancer ; Pancreatic Neoplasms ; Pancreatic Neoplasms - drug therapy ; Patient outcomes ; Peripheral Nervous System Diseases - chemically induced ; Peripheral Nervous System Diseases - therapy ; Polyneuropathies ; Quality of Life ; Risk Factors</subject><ispartof>Oncology, 2022-07, Vol.100 (7), p.384-391</ispartof><rights>2022 S. Karger AG, Basel</rights><rights>2022 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2022 S. Karger AG</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-c872e0c96080c0d5c83f873a94a1b000bfb42fe70586a52870f3a21b57e199703</citedby><cites>FETCH-LOGICAL-c467t-c872e0c96080c0d5c83f873a94a1b000bfb42fe70586a52870f3a21b57e199703</cites><orcidid>0000-0003-1856-2848</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,2430,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35551139$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Catalano, Martina</creatorcontrib><creatorcontrib>Ramello, Monica</creatorcontrib><creatorcontrib>Conca, Raffaele</creatorcontrib><creatorcontrib>Aprile, Giuseppe</creatorcontrib><creatorcontrib>Petrioli, Roberto</creatorcontrib><creatorcontrib>Roviello, Giandomenico</creatorcontrib><title>Risk Factors for Nab-Paclitaxel and Gemcitabine-Induced Peripheral Neuropathy in Patients with Pancreatic Cancer</title><title>Oncology</title><addtitle>Oncology</addtitle><description>Background: Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most frequent adverse events observed with taxane use, whose disability often required modification or treatment discontinuation. The aim of this study was to assess the value of several variables as risk factors for CIPN development. Material and Methods: Eligible patients with metastatic pancreatic cancer receiving chemotherapy with nab-paclitaxel and gemcitabine were assessed in a multicenter study. Peripheral neuropathy was categorized using the National Cancer Institute Common Toxicity Criteria scale, version 4.02, and a physical/neurological examination. Univariate and multivariate regression analyses were used to identify blood-based and clinical factors associated with CIPN. Results: Data were available from 153 patients from five Italian centers. Key risk factors of CIPN in univariate regression models included age, number of chemotherapy cycles, statin assumption, and concomitant comorbidities. However, in the multivariate analysis, only for age (OR 1.0, p < 0.01, 95% CI: 1.01–1.11) and the number of cycles (OR 1.22, p < 0.01, 95% CI: 1.09–1.36), the correlation with CIPN development has been confirmed. Conclusion: Our study confirms age and the number of chemotherapy cycles as CIPN risk factors. The identification and validation of different risk factors could be advantageous to prevent or optimize management of CIPN which outstandingly affect the patient’s quality of life.</description><subject>Albumins</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Care and treatment</subject><subject>Clinical Study</subject><subject>Complications and side effects</subject><subject>Deoxycytidine - analogs & derivatives</subject><subject>Gemcitabine</subject><subject>Humans</subject><subject>Paclitaxel</subject><subject>Paclitaxel - adverse effects</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Patient outcomes</subject><subject>Peripheral Nervous System Diseases - chemically induced</subject><subject>Peripheral Nervous System Diseases - therapy</subject><subject>Polyneuropathies</subject><subject>Quality of Life</subject><subject>Risk Factors</subject><issn>0030-2414</issn><issn>1423-0232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0VFr1TAUB_AgirtOH3wXCQwEHzpPkqZpH8fFzcFlu4g-lzQ9WePatCS56L69kerFwchDck5-_0A4hLxlcM6YbD4BgORlXdXPyIaVXBTABX9ONgACCl6y8oS8ivFHZkqW1UtyIqSUjIlmQ5avLt7TS23SHCK1c6A3uiv22owu6V84Uu17eoWTyWXnPBbXvj8Y7Okeg1sGDHqkN3gI86LT8ECdp3udHPoU6U-Xhlx5EzC3DN3mI4bX5IXVY8Q3f_dT8v3y87ftl2J3e3W9vdgVpqxUKkytOIJpKqjBQC9NLWythG5Kzbr8kc52JbeoQNaVlrxWYIXmrJMKWdMoEKfkbH33To_YOm_nFLSZXDTthYKmAV41VVbnT6i8epycmT1al_uPAh_-CwyoxzTEeTwkN_v4GH5coQlzjAFtuwQ36fDQMmj_TK09Ti3b96tdDt2E_VH-G1MG71Zwr8MdhiM45s-evL7d7lbRLr0VvwE1iKRi</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Catalano, Martina</creator><creator>Ramello, Monica</creator><creator>Conca, Raffaele</creator><creator>Aprile, Giuseppe</creator><creator>Petrioli, Roberto</creator><creator>Roviello, Giandomenico</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-1856-2848</orcidid></search><sort><creationdate>20220701</creationdate><title>Risk Factors for Nab-Paclitaxel and Gemcitabine-Induced Peripheral Neuropathy in Patients with Pancreatic Cancer</title><author>Catalano, Martina ; Ramello, Monica ; Conca, Raffaele ; Aprile, Giuseppe ; Petrioli, Roberto ; Roviello, Giandomenico</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-c872e0c96080c0d5c83f873a94a1b000bfb42fe70586a52870f3a21b57e199703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Albumins</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Care and treatment</topic><topic>Clinical Study</topic><topic>Complications and side effects</topic><topic>Deoxycytidine - analogs & derivatives</topic><topic>Gemcitabine</topic><topic>Humans</topic><topic>Paclitaxel</topic><topic>Paclitaxel - adverse effects</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Patient outcomes</topic><topic>Peripheral Nervous System Diseases - chemically induced</topic><topic>Peripheral Nervous System Diseases - therapy</topic><topic>Polyneuropathies</topic><topic>Quality of Life</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Catalano, Martina</creatorcontrib><creatorcontrib>Ramello, Monica</creatorcontrib><creatorcontrib>Conca, Raffaele</creatorcontrib><creatorcontrib>Aprile, Giuseppe</creatorcontrib><creatorcontrib>Petrioli, Roberto</creatorcontrib><creatorcontrib>Roviello, Giandomenico</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Catalano, Martina</au><au>Ramello, Monica</au><au>Conca, Raffaele</au><au>Aprile, Giuseppe</au><au>Petrioli, Roberto</au><au>Roviello, Giandomenico</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk Factors for Nab-Paclitaxel and Gemcitabine-Induced Peripheral Neuropathy in Patients with Pancreatic Cancer</atitle><jtitle>Oncology</jtitle><addtitle>Oncology</addtitle><date>2022-07-01</date><risdate>2022</risdate><volume>100</volume><issue>7</issue><spage>384</spage><epage>391</epage><pages>384-391</pages><issn>0030-2414</issn><eissn>1423-0232</eissn><abstract>Background: Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most frequent adverse events observed with taxane use, whose disability often required modification or treatment discontinuation. The aim of this study was to assess the value of several variables as risk factors for CIPN development. Material and Methods: Eligible patients with metastatic pancreatic cancer receiving chemotherapy with nab-paclitaxel and gemcitabine were assessed in a multicenter study. Peripheral neuropathy was categorized using the National Cancer Institute Common Toxicity Criteria scale, version 4.02, and a physical/neurological examination. Univariate and multivariate regression analyses were used to identify blood-based and clinical factors associated with CIPN. Results: Data were available from 153 patients from five Italian centers. Key risk factors of CIPN in univariate regression models included age, number of chemotherapy cycles, statin assumption, and concomitant comorbidities. However, in the multivariate analysis, only for age (OR 1.0, p < 0.01, 95% CI: 1.01–1.11) and the number of cycles (OR 1.22, p < 0.01, 95% CI: 1.09–1.36), the correlation with CIPN development has been confirmed. Conclusion: Our study confirms age and the number of chemotherapy cycles as CIPN risk factors. The identification and validation of different risk factors could be advantageous to prevent or optimize management of CIPN which outstandingly affect the patient’s quality of life.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>35551139</pmid><doi>10.1159/000524868</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1856-2848</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Albumins Antineoplastic Agents - adverse effects Care and treatment Clinical Study Complications and side effects Deoxycytidine - analogs & derivatives Gemcitabine Humans Paclitaxel Paclitaxel - adverse effects Pancreatic cancer Pancreatic Neoplasms Pancreatic Neoplasms - drug therapy Patient outcomes Peripheral Nervous System Diseases - chemically induced Peripheral Nervous System Diseases - therapy Polyneuropathies Quality of Life Risk Factors |
title | Risk Factors for Nab-Paclitaxel and Gemcitabine-Induced Peripheral Neuropathy in Patients with Pancreatic Cancer |
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